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Device Image Artifact Evaluation Result
The unacceptable distortion of an image due to signal loss that may occur during a radiologic procedure such as magnetic resonance imaging. (Food and Drug Administration)
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A subject domain utilized for the submission of information encompassing and representing data, vocabulary or records related to device identifiers.
Testing the device's protective materials to prevent moisture penetration or ingress.
A device that malfunctions as the result of exposure to undesirable levels of humidity
Testing the device for its affect or impact on the blood or its components.
The device affects or impacts the blood or its components. (See ISO 10993)
A problem that results from improper sequencing or activation of electronic components.
